ライフサイエンスコーパス: intestinal content

1 ence analysis of bacterial DNA prepared from intestinal content.

2 tion of nitroso compounds in feces and small intestinal content.

3 l in milieus that mimicked gastric and small intestinal content.

4 er followed by the lungs, breasts, and small intestinal content.

5 and proteolytic activities were measured in intestinal contents.

6 were also evaluated to simulate postprandial intestinal contents.

7 n drinking water) led to alkalization of the intestinal contents.

8 ISA, and PEC was detected by IEM in feces or intestinal contents.

9 physical barrier between the host tissue and intestinal contents, a separation that is vital for heal

10 raises the possibility that dysbiosis of the intestinal content also influences the outcome of cancer

11 layer and higher Listeria loads both in the intestinal content and deeper tissues compared to WT Lis

12 Enteroendocrine cells (EECs) sense intestinal content and release hormones to regulate gast

13 hese transitions include dramatic changes in intestinal contents and require appropriate adaptations

14 a physical and chemical barrier between the intestinal contents and the underlying epithelia.

15 in net fluid hyperabsorption, dehydration of intestinal contents, and a propensity to inspissated int

16 le patient cohorts, in mouse small and large intestinal contents, and in patient-derived ex vivo comm

17 ton pump inhibitors in simulated stomach and intestinal contents, as well as comparing name-brand and

18 The metabolomic profiles of the intestinal contents, biofluids, and several tissues invo

19 a, and lower viral loads in liver, bile, and intestinal content collected at three different necropsy

20 eritoneal infection after contamination with intestinal contents during surgery.

21 ification of bile acids as active factors in intestinal content fluid essential for PEC growth.

22 LLC-PK cells, but only in the presence of an intestinal content fluid filtrate from gnotobiotic pigs.

23 Serial dilutions of intestinal contents from adult male rats were plated on

24 tected by immunoelectron microscopy (IEM) in intestinal contents from all the WT-PEC-inoculated pigs,

25 their characterization, mass spectrometry of intestinal contents from gnotobiotic mice, plus in vitro

26 Analyses of intestinal contents from mice revealed alcohol-associate

27 Pigs inoculated intravenously with serum or intestinal contents from the viremic virulent HRV-inocul

28 n cell culture but only with the addition of intestinal contents from uninfected gnotobiotic pigs.

29 ted were abdominal fluid (dogs and cats) and intestinal contents (horses).

30 om physiologic polymicrobial cultures (e.g., intestinal contents, human feces) and reduce TMAO levels

31 I/4/HS66/2001/US strain or with pig-passaged intestinal contents (IC) and euthanized acutely (n = 43)

32 rofiles were determined in serum, feces, and intestinal contents (IC) of the HuNoV-HS66-inoculated ca

33 (reg)] IL-10) cytokine profiles in serum and intestinal contents (IC) of the HuNoV-HS66-inoculated pi

34 tion in hilA or invG were recovered from the intestinal contents, intestinal tissues, and systemic ti

35 r V. cholerae The induction of TCP by murine intestinal contents is counteracted when Ca(2+) is deple

36 levels in the liver, intestine, plasma, and intestinal content, led to drastic decreases in the mRNA

37 MS/MS), PCB52 was present in adipose, brain, intestinal content, lung, liver, and serum.

38 g or infectious virus titers in the feces or intestinal contents measured by enzyme-linked immunosorb

39 t for ESBL-producing Escherichia coli in the intestinal content of treated dairy cows and in manure s

40 n this study, U.S. PDCoV strain OH-FD22 from intestinal contents of a diarrheic pig from Ohio was iso

41 ain, PC177, by blind serial passaging of the intestinal contents of a diarrheic piglet in Vero cell c

42 D patients and mice, as well as in liver and intestinal contents of NAFLD mice compared to their heal

43 zyme-linked immunosorbent assay in serum and intestinal contents of neonatal gnotobiotic pigs and IL-

44 [OH-FD22(DC44) strain] in LLC-PK cells from intestinal contents of PDCoV OH-FD22 strain-inoculated g

45 nt IFN-gamma responses occurred in serum and intestinal contents of the AttHRV-infected pigs, compare

46 The feces or intestinal contents of the cows and inoculated calves we

47 ed with wild-type mice, but their vitamin K1 intestinal content remained unchanged.

48 at protects mammals from potentially harmful intestinal contents, such as pathogenic bacteria.

49 rete different molecules in their saliva and intestinal content that counteract host defences and hel

50 mune response predisposes to accumulation of intestinal contents that breach the mucosal barrier of t

51 uring vortex mixing and downward flow of the intestinal contents, thereby persisting long enough for

52 modify hepatic homeostatic pathways, linking intestinal content to metabolic activity.

53 Levels of breath hydrogen were measured and intestinal content was assessed by MRI before and at var

54 5-HT intestinal content was measured using immunohistochemist

55 Vitamin D and K intestinal contents were also reduced in mice force-fed

56 The convergence of endocrine and intestinal contents within PLNs has significant implicat